Literature DB >> 11856034

Arabinofuranosides from mycobacteria: synthesis of a highly branched hexasaccharide and related fragments containing beta-arabinofuranosyl residues.

Haifeng Yin1, Francis W D'Souza, Todd L Lowary.   

Abstract

The synthesis of 11 oligosaccharides (4-14) containing beta-arabinofuranosyl residues is reported. The glycans are all fragments of two polysaccharides, arabinogalactan and lipoarabinomannan, which are found in the cell wall complex of mycobacteria. In the preparation of the targets, the key step was a low-temperature glycosylation reaction that installed the beta-arabinofuranosyl residues with good to excellent stereocontrol.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11856034     DOI: 10.1021/jo010910e

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  9 in total

1.  Stereospecific Furanosylations Catalyzed by Bis-thiourea Hydrogen-Bond Donors.

Authors:  Andrew B Mayfield; Jan B Metternich; Adam H Trotta; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2020-02-14       Impact factor: 15.419

2.  Stereoselective 1,2-cis Furanosylations Catalyzed by Phenanthroline.

Authors:  Hengfu Xu; Richard N Schaugaard; Jiayi Li; H Bernhard Schlegel; Hien M Nguyen
Journal:  J Am Chem Soc       Date:  2022-04-12       Impact factor: 16.383

3.  Synthesis and immunogenicity of the Mycobacterium tuberculosis arabinomannan-CRM197 conjugate.

Authors:  Yunsong Chang; Xin Meng; Yaxin Li; Jianmei Liang; Tingshen Li; Demei Meng; Tao Zhu; Peng Yu
Journal:  Medchemcomm       Date:  2019-04-02       Impact factor: 3.597

4.  Antigen 85C-mediated acyl-transfer between synthetic acyl donors and fragments of the arabinan.

Authors:  Aditya K Sanki; Julie Boucau; Donald R Ronning; Steven J Sucheck
Journal:  Glycoconj J       Date:  2008-12-04       Impact factor: 2.916

5.  On the use of 3,5-O-benzylidene and 3,5-O-(di-tert-butylsilylene)-2-O-benzylarabinothiofuranosides and their sulfoxides as glycosyl donors for the synthesis of beta-arabinofuranosides: importance of the activation method.

Authors:  David Crich; Christian Marcus Pedersen; Albert A Bowers; Donald J Wink
Journal:  J Org Chem       Date:  2007-02-08       Impact factor: 4.354

6.  Molecular basis of arabinobio-hydrolase activity in phytopathogenic fungi: crystal structure and catalytic mechanism of Fusarium graminearum GH93 exo-alpha-L-arabinanase.

Authors:  Raphaël Carapito; Anne Imberty; Jean-Marc Jeltsch; Simon C Byrns; Pui-Hang Tam; Todd L Lowary; Annabelle Varrot; Vincent Phalip
Journal:  J Biol Chem       Date:  2009-03-06       Impact factor: 5.157

7.  Synthesis of a tetra- and a trisaccharide related to an anti-tumor saponin "Julibroside J28" from Albizia julibrissin.

Authors:  Bimalendu Roy; Kausikisankar Pramanik; Balaram Mukhopadhyay
Journal:  Glycoconj J       Date:  2007-08-16       Impact factor: 2.916

8.  Synthesis of a miniature lipoarabinomannan.

Authors:  Jian Gao; Guochao Liao; Lizhen Wang; Zhongwu Guo
Journal:  Org Lett       Date:  2014-01-21       Impact factor: 6.005

9.  Twenty Years of Mycobacterial Glycans: Furanosides and Beyond.

Authors:  Todd L Lowary
Journal:  Acc Chem Res       Date:  2016-06-13       Impact factor: 22.384

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.